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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094093copy number variation2nstd102humanUncertain significance GRCh37 chr11: 64,973,914-70,052,579 , GRCh38.p12 chr11: 65,206,443-70,206,473 B4GAT1, CHKA-DT, 208 more genes
    nsv6914093copy number variation1nstd229human GRCh38 chr11: 66,282,766-66,295,500 , GRCh37.p13 chr11: 66,050,237-66,062,971 YIF1A, CNIH2, 1 more genes
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6621258copy number variation1nstd224human GRCh37 chr11: 66,055,077-66,066,664 , GRCh38.p12 chr11: 66,287,606-66,299,193 YIF1A, TMEM151A
    nsv6459699copy number variation1nstd223human GRCh38 chr11: 66,294,079-66,294,458 , GRCh37.p13 chr11: 66,061,550-66,061,929 TMEM151A
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6314192copy number variation1nstd102humanUncertain significance GRCh37 chr11: 64,935,724-66,405,514 , GRCh38.p12 chr11: 65,168,253-66,638,043 CNIH2, GAL3ST3, 95 more genes
    nsv6309121copy number variation2nstd102humanPathogenic GRCh37 chr11: 64,522,783-66,283,694 , GRCh38.p12 chr11: 64,755,311-66,516,223 SF3B2, ZNRD2-DT, 124 more genes
    nsv6290938copy number variation1nstd102humanUncertain significance GRCh37 chr11: 65,963,737-66,581,485 , GRCh38.p12 chr11: 66,196,266-66,814,014 CCS, RN7SL12P, 38 more genes
    nsv6132271copy number variation1nstd213human GRCh37 chr11: 66,040,000-66,380,001 , GRCh38.p12 chr11: 66,272,529-66,612,530 BBS1, YIF1A, 24 more genes
    nsv6132112copy number variation1nstd213human GRCh37 chr11: 64,220,000-68,010,001 , GRCh38.p12 chr11: 64,452,528-68,242,533 ACTN3, ALDH3B1, 212 more genes
    nsv6031209copy number variation1nstd212human GRCh37.p13 chr11: 66,023,643-66,066,070 , GRCh38 chr11: 66,256,172-66,298,599 YIF1A, KLC2, 6 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5277798copy number variation1nstd204human GRCh38.p13 chr11: 65,676,501-66,823,500 , GRCh37.p13 chr11: 65,443,972-66,590,971 , BBS1, 68 more genes
    nsv5265802copy number variation1nstd204human GRCh38.p13 chr11: 66,289,020-66,291,419 , GRCh37.p13 chr11: 66,056,491-66,058,890 YIF1A, TMEM151A
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4453555copy number variation1nstd102humanUncertain significance GRCh38 chr11: 65,866,431-66,347,555 , GRCh37 chr11: 65,633,902-66,115,026 CNIH2, YIF1A, 33 more genes
    nsv4349000copy number variation1nstd102humanPathogenic GRCh37 chr11: 65,138,976-67,574,402 , GRCh38.p12 chr11: 65,371,505-67,806,931 SNORD13F, ZNRD2, 141 more genes
    nsv4197804copy number variation1nstd166human GRCh37.p13 chr11: 66,058,687-66,058,763 , GRCh38.p12 chr11: 66,291,216-66,291,292 TMEM151A
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